Drug profile

The FDA adverse-event record for Unknown If Any Concomitant Medications

42 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Unknown If Any Concomitant Medications. Species, reactions, and outcomes follow.

#1233 of 2,679
by report volume (all drugs)
42
adverse-event reports
26.2%
death-coded share
Dog
most-reported species

Corpus placement

According to the FDA Center for Veterinary Medicine openFDA adverse-event extract, Unknown If Any Concomitant Medications ranks #1222 of 2679 by total reports (42). Death-coded-share rank requires at least 50 reports. National dual: Milbemycin Oxime + Spinosad is #1 of 2679 drugs by total adverse-event reports (149,624) at death-coded-share rank 965 of 1130 drugs with at least 50 reports (2.3%); separately, Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) is #1 highest death-coded share at 97.8% (report rank #821).

149,624
Milbemycin Oxime + Spinosad reports (#1)
97.8%
Atlantic Salmon Transgenic Whole (Opafp-Ghc2 Rdna Construct Inserted Into The A-Locus In The Eo-1A Lineage) death share (#1)
#1222
This drug, reports of 2679

Report volume reflects how common a breed or drug is and how often owners and vets file — not actual risk. Death-coded share ranks are limited to entries with enough reports to be meaningful. The two maps do not agree at #1.

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Unknown If Any Concomitant Medications has 42 reports now versus 42 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
Death-coded reports
+0
Death-coded share
−0.0 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Unknown If Any Concomitant Medications changes

Signature read: Unknown If Any Concomitant Medications's 26.2% death-coded share is among the highest in the openFDA drug corpus.

Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
42
Total Reports
11
Deaths Reported
26.2%
Death-coded share of reports

Active Ingredients

Unknown If Any Concomitant Medications

Administration Routes

Unknown

Species Affected

Dog 39
Cat 3

Most Affected Breeds

Dog (unknown) 7
Rottweiler 5
Spitz - German Pomeranian 4
Chihuahua 3
Retriever - Labrador 3
Dachshund - Miniature 2
Cat (unknown) 2
Boxer (German Boxer) 2
Collie - Border 2
Terrier - Yorkshire 1

Most Reported Reactions

Death 9
Emesis 5
Behavioural disorder NOS 4
Seizure NOS 4
Anaemia NOS 4
Pale mucous membrane 4
Lack of efficacy (ectoparasite) - flea 4
Emesis (multiple) 3
Ataxia 3
Foaming at the mouth 3
NT - Abnormal necropsy finding NOS 3
Anorexia 2

Outcome Breakdown

Ongoing
13 (31.0%)
Recovered/Normal
10 (23.8%)
Died
9 (21.4%)
Outcome Unknown
7 (16.7%)
Euthanized
2 (4.8%)
Recovered with Sequela
1 (2.4%)

Unknown If Any Concomitant Medications: high death-coded share in the FDA AER row

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

What to do with this drug

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Unknown If Any Concomitant Medications (#1233 of 2,679 by report volume); death-coded 26.2%. PlainBreed drug row · death-coded share stamp 26.2% · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →